Health beliefs as a predictor of screening behaviors among college students

References

• Alford, S. H., McBride, C. M., Reid, R. J., Larson, E. B., Baxevanis, A. D., & Brody, L. C. (2011). Participation in genetic testing research varies by social group. Public Health Genomics, 14(2), 85–93. doi:10.1159/000294277
   PubMed Web of Science ®Google Scholar
• American Society of Hematology [ASH]. (2017). The state of sickle cell disease: 2016 report (2016, amended effective August 9, 2017). Retrived from scdcoalition.org/pdfs/ASH%20State%20of%20Sickle%20Cell%20Disease%202016%20Report.pdf
   Google Scholar
• Asnani, M. R., Quimby, K. R., Bennett, N. R., & Francis, D. K. (2016). Interventions for patients and caregivers to improve knowledge of sickle cell disease and recognition of its related complications. Cochrane Database of Systematic Reviews, 2016(10). doi:10.1002/14651858.CD011175.pub2
   Google Scholar
• Bediako, S. M., & Moffitt, K. R. (2011). Race and social attitudes about sickle cell disease. Ethnicity & Health, 16(4–5), 423–429. doi:10.1080/13557858.2011.552712
   PubMed Web of Science ®Google Scholar
• Benson, J. M., & Therrell, B. L. (2010). History and current status of newborn screening for hemoglobinopathies.Seminars in Perinatology, 34(2),134–144. doi:10.1053/j.semperi.2009.12.006
   PubMed Web of Science ®Google Scholar
• Bhatt, K., Reid, M. E., Lewis, N. A., & Asnani, M. R. (2011). Knowledge and health beliefs of Jamaican adolescents with sickle cell disease. Pediatric Blood & Cancer, 57(6), 1044–1048. doi:10.1002/pbc.23091
   PubMed Web of Science ®Google Scholar
• Bulgin, D., Tanabe, P., & Jenerette, C. (2018). Stigma of sickle cell disease: A systematic review.Issues in Mental Health Nursing, 39(8),675–686. doi:10.1080/01612840.2018.1443530
   PubMed Web of Science ®Google Scholar
• Centers for Disease Control and Prevention [CDC]. (2015). What you should know about sickle cell trait. Retrived fromhttp://www.cdc.gov/ncbddd/sicklecell/documents/factsheet_sickle_cell_trait.pdf
   Google Scholar
• Centers for Disease Control and Prevention [CDC]. (2017). Data & statistics on sickle cell disease. Retrived from http://www.cdc.gov/ncbddd/sicklecell/data.html
   Google Scholar
• Chai, Y., Coloigner, J., Qu, X., Choi, S., Bush, A., Borzage, M., … Wood, J. (2015, November 17-19). Tract specific analysis in patients with sickle cell disease. [Proceedings v.968108]. 11th International Symposium on Medical Information Processing and Analysis, Cuenca, Ecuador. doi:10.1117/12.2213617
   Google Scholar
• Creary, S., Adan, I., Stanek, J., O’Brien, S. H., Chisolm, D. J., Jeffries, T., … Varga, E. (2017). Sickle cell trait knowledge and health literacy in caregivers who receive in‐person sickle cell trait education. Molecular Genetics & Genomic Medicine, 5(6), 692–699. doi:10.1002/mgg3.327
   PubMed Web of Science ®Google Scholar
• Gallo, A. M., Wilkie, D., Suarez, M., Labotka, R., Molokie, R., Thompson, A., … Johnson, B. (2010). Reproductive decisions in people with sickle cell disease or sickle cell trait. Western Journal of Nursing Research, 32(8), 1073–1090. doi:10.1177/0193945910371482
   PubMed Web of Science ®Google Scholar
• Gustafson, S. L., Gettig, E. A., Watt-Morse, M., & Krishnamurti, L. (2007). Health beliefs among African American women regarding genetic testing and counseling for sickle cell disease. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 9(5), 303–310. doi:10.1097/GIM.0b013e3180534282
   PubMed Web of Science ®Google Scholar
• Guvenc, G., Akyuz, A., & Acikel, C. H. (2011). Health belief model scale for cervical cancer and pap smear test: Psychometric testing. Journal of Advanced Nursing, 67(2), 428–437. doi:10.1111/j.1365-2648.2010.05450.xc
   PubMed Web of Science ®Google Scholar
• Jones, C. J., Smith, H., & Llewellyn, C. (2014). Evaluating the effectiveness of Health Belief Model interventions in improving adherence: A systematic review. Health Psychology Review, 8(3), 253–269. doi:10.1080/17437199.2013.802623
   PubMed Web of Science ®Google Scholar
• Kavanagh, P. L., Wang, C. J., Therrell, B. L., Sprinz, P. G., & Bauchner, H. (2008). Communication of positive newborn screening results for sickle cell disease and sickle cell trait: Variation across states. American Journal of Medical Genetics, 148c(1), Part C, Seminars in Medical Genetics, 15–22. doi:10.1002/ajmg.c.30160
   PubMed Web of Science ®Google Scholar
• Kia, N. S., Karami, K., Mohamadian, H., & Malehi, A. (2018). Evaluation of an educational intervention based on health belief model on beta thalassemia carrier and final suspects couples. Journal of Education and Health Promotion, 7(1), 77. doi:10.4103/jehp.jehp_103_16
   PubMedGoogle Scholar
• Lee, L., Smith-Whitley, K., Banks, S., & Puckrein, G. (2019). Reducing health care disparities in sickle cell disease: A review. Public Health Reports, 134(6), 599–607. doi:10.1177/0033354919881438
   PubMed Web of Science ®Google Scholar
• Livingston, G., & Brown, A. (2017). Intermarriage in the US 50 Years After Loving v. Virginia. Pew Research Center. Retrived from https://www.pewsocialtrends.org/2017/05/18/intermarriage-in-the-u-s-50-years-after-loving-v-virginia/
   Google Scholar
• Long, K. A., Thomas, S. B., Grubs, R. E., Gettig, E. A., & Krishnamurti, L. (2011). Attitudes and beliefs of African-Americans toward genetics, genetic testing, and sickle cell disease education and awareness. Journal of Genetic Counseling, 20(6), 572–592. doi:10.1007/s10897-011-9388-3
   PubMed Web of Science ®Google Scholar
• Mayo-Gamble, T. L., Barnes, P. A., Cunningham Erves, J., Middlestadt, S. E., & Lin, H. (2018a). ‘It means everyone should know their status’: Exploring lay conceptions of sickle cell trait and sickle cell trait screening among African Americans within middle reproductive age.Ethnicity & Health,23(7),813–829. doi:10.1080/13557858.2017.1295135
   PubMed Web of Science ®Google Scholar
• Mayo-Gamble, T. L., Middlestadt, S. E., Lin, H., Cunningham-Erves, J., Barnes, P., & Jackson, P. B. (2018b). Identifying factors underlying the decision for sickle cell carrier screening among African Americans within middle reproductive age. Journal of Genetic Counseling, 27(5), 1302–1311. doi:10.1007/s10897-018-0255-3
   PubMed Web of Science ®Google Scholar
• Mayo‐Gamble, T. L., Schlundt, D., Cunningham‐Erves, J., Murry, V. M., Bonnet, K., Quasie‐Woode, D., & Mouton, C. P. (2019). Sickle cell carriers’ unmet information needs: Beyond knowing trait status.Journal of Genetic Counseling,28(4),812–821. doi:10.1002/jgc4.1124
   PubMed Web of Science ®Google Scholar
• Molina-Barceló, A., Salas Trejó, D., Peiró-Pérez, R., & Málaga López, A. (2011). To participate or not? Giving voice to gender and socio-economic differences in colorectal cancer screening programmes. European Journal of Cancer Care, 20(5), 669–678. doi:10.1111/j.1365-2354.2011.01263.x
   PubMed Web of Science ®Google Scholar
• National Association of Social Workers [NASW]. (2019). Read the code of ethics. Retrived from https://www.socialworkers.org/About/Ethics/Code-of-Ethics/Code-of-Ethics-English
   Google Scholar
• National Cancer Institute [NCI]. (2005). Theory at a glance: A guide for health promotion practice. National Institute of Health, NIH Publication No. xx-xxxx.
   Google Scholar
• National Heart, Lung, and Blood Institute [NHLBI]. (2018). Diseases and conditions index- sickle cell disease: Causes. US Department of Health and Human Services. Retrived from https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease
   Google Scholar
• Nelson, S. C., & Hackman, H. W. (2013). Race matters: Perceptions of race and racism in a sickle cell center. Pediatric Blood & Cancer, 60(3), 451–454. doi:10.1002/pbc.24361
   PubMed Web of Science ®Google Scholar
• Nordentoft, M. (2011). Crucial element in suicide prevention strategies. Progress in Neuro-Psychopharmacology & Biological Psychiatry, 35(4), 848–853. doi:10.1016/j.pnpbp.2010.11.038
   PubMed Web of Science ®Google Scholar
• Ojodu, J., Hulihan, M. M., Pope, S. N., & Grant, A. M. (2014). Incidence of sickle cell trait – United States 2010. Centers for Disease Control and Prevention. Morbidity and Mortality Weekly Report, 63(49), 1155–1158. https://www.cdc.gov/mmWr/preview/mmwrhtml/mm6349a3.htm
   PubMed Web of Science ®Google Scholar
• Olatona, F. A., Odeyemi, K. A., Onajole, A. T., & Asuzu, M. C. (2012). Effects of health education on knowledge and attitude of youth corps members to sickle cell disease and its screening in Lagos State. Community Medicine & Health Education, 2(7), 1–6. doi:10.4172/2161-0711.1000163
   Google Scholar
• Owolabi, R. S., Alabi, P., Daniel, O., Ajayi, S., Otu, T., & Ogundiran, A. (2011). Knowledge and attitudes of secondary school students in federal capital territory (FCT), Abuja, Nigeria towards sickle cell disease. Nigerian Journal of Medicine: Journal of the National Association of Resident Doctors of Nigeria, 20(4), 479.
   PubMedGoogle Scholar
• Piel, F. B., Hay, S. I., Gupta, S., Weatherall, D. J., & Williams, T. N. (2013). Global burden of sickle cell anaemia in children under five, 2010-2050: Modelling based on demographics, excess mortality, and interventions. PLoS Medicine, 10(7), e1001484. doi:10.1371/journal.pmed.1001484
   PubMed Web of Science ®Google Scholar
• Piel, F. B., Patil, A. P., Howes, R. E., Nyangiri, O. A., Gething, P. W., Dewi, M., … Hay, S. I. (2012). Global epidemiology of sickle haemoglobin in neonates: A contemporary geostatistical model-based map and population estimates. The Lancet, 381(9861), 142–151. doi:10.1016/S0140-6736(12)61229-X
   PubMed Web of Science ®Google Scholar
• Rosenstock, I. M. (1974). Historical origins of the health belief model. Health Education Monographs, 2(4), 328–335. doi:10.1177/109019817400200403
   Google Scholar
• Ross, P. T. (2015). Motivations of women with sickle cell disease for asking their partners to undergo genetic testing. Social Science & Medicine, 139, 36–43. doi:10.1016/j.socscimed.2015.06.029
   PubMed Web of Science ®Google Scholar
• Sickle Cell Disease Association of America [SCDAA]. (2012). Research and screening. Retrived from http://www.sicklecelldisease.org/index.cfm?page=about-scd
   Google Scholar
• Sickle Cell Disease Association of America [SCDAA]. (2018). Community health worker training. Retrived from https://www.sicklecelldisease.org/our-initiatives/community-health-worker-training
   Google Scholar
• Smith, M., & Aguirre, R. T. P. (2012). Reproductive attitudes and behaviors in people with sickle cell disease or sickle cell trait: A qualitative interpretive meta-synthesis. Social Work in Health Care, 51(9), 757–779. doi:10.1080/00981389.2012.693580
   PubMed Web of Science ®Google Scholar
• Smith, M., & Brownell, G. (2018). Knowledge, beliefs, attitudes, and behaviors regarding sickle cell disease: Implications for prevention. Social Work in Public Health, 33(5), 299–316. doi:10.1080/19371918.2018.1469064
   PubMed Web of Science ®Google Scholar
• Substance Abuse and Mental Health Services Administration’s [SAMHSA], (2016). Primary, secondary and tertiary prevention strategies & interventions for preventing NMUPD and opioid overdose across the IOM continuum of care. Center for the Application of Prevention Technologies. Retrived from https://www.edc.org/center-application-prevention-technologies-capt
   Google Scholar
• Texas Department of State Health Services [TDSHS]. (2012). Universal, selective, and indicated prevention. Retrived from http://www.dshs.state.tx.us/sa/prevention/classifications.shtm
   Google Scholar
• Treadwell, M. J., McClough, L., & Vichinsky, E. (2006). Using qualitative and quantitative strategies to evaluate knowledge and perceptions about sickle cell disease and sickle cell trait. Journal of the National Medical Association, 98(5), 704–710.
   PubMed Web of Science ®Google Scholar
• Ugwu, N. I. (2016). Pre-marital screening for sickle cell hemoglobin and genetic counseling: Awareness and acceptability among undergraduate students of a Nigerian University. International Journal of Medicine & Biomedical Research, 5(1), 43–49. doi:10.14194/ijmbr.5.1.6
   Google Scholar
• United States Census Bureau [USCB]. (2012). 2010 Census Shows Interracial and Interethnic Married Couples Grew by 28 Percent over Decade. Retrived from https://www.census.gov/newsroom/releases/archives/2010_census/cb12-68.html
   Google Scholar
• United States Department of Health and Human Services, National Institutes of Health [US-DHHS, NIH]. (2010). Sickle cell disease awareness and education strategy development workshop report. Bethesda, MD: National Heart, Lung, and Blood Institute. Retrived from https://www.nhlbi.nih.gov/health-topics/all-publications-andresources/sickle-cell-disease-awareness-and-educationstrategy.
   Google Scholar
• Vichinsky, E. P. (2014). Sickle cell trait. Retrived from http://www.uptodate.com/contents/sickle-cell-trait.
   Google Scholar
• World Health Organization [WHO]. (2011). Statement of the Regional Director at the opening of the Regional Ministerial Consultation on Noncommunicable Diseases, Brazzaville, Congo. Regional Office for Africa. Retrived from https://www.afro.who.int/regional-director/speeches-messages/statement-regional-director-opening-regional-ministerial
   Google Scholar